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J Cell Physiol ; 216(3): 583-94, 2008 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18330887

RESUMO

We are investigating effects of the depsipeptide geodiamolide H, isolated from the Brazilian sponge Geodia corticostylifera, on cancer cell lines grown in 3D environment. As shown previously geodiamolide H disrupts actin cytoskeleton in both sea urchin eggs and breast cancer cell monolayers. We used a normal mammary epithelial cell line MCF 10A that in 3D assay results formation of polarized spheroids. We also used cell lines derived from breast tumors with different degrees of differentiation: MCF7 positive for estrogen receptor and the Hs578T, negative for hormone receptors. Cells were placed on top of Matrigel. Spheroids obtained from these cultures were treated with geodiamolide H. Control and treated samples were analyzed by light and confocal microscopy. Geodiamolide H dramatically affected the poorly differentiated and aggressive Hs578T cell line. The peptide reverted Hs578T malignant phenotype to polarized spheroid-like structures. MCF7 cells treated by geodiamolide H exhibited polarization compared to controls. Geodiamolide H induced striking phenotypic modifications in Hs578T cell line and disruption of actin cytoskeleton. We investigated effects of geodiamolide H on migration and invasion of Hs578T cells. Time-lapse microscopy showed that the peptide inhibited migration of these cells in a dose-dependent manner. Furthermore invasion assays revealed that geodiamolide H induced a 30% decrease on invasive behavior of Hs578T cells. Our results suggest that geodiamolide H inhibits migration and invasion of Hs578T cells probably through modifications in actin cytoskeleton. The fact that normal cell lines were not affected by treatment with geodiamolide H stimulates new studies towards therapeutic use for this peptide.


Assuntos
Neoplasias da Mama/patologia , Técnicas de Cultura de Células , Movimento Celular/efeitos dos fármacos , Citoesqueleto/efeitos dos fármacos , Depsipeptídeos/farmacologia , Invasividade Neoplásica , Células Tumorais Cultivadas/efeitos dos fármacos , Actinas/metabolismo , Animais , Apoptose , Materiais Biocompatíveis/metabolismo , Linhagem Celular , Polaridade Celular , Forma Celular , Colágeno/metabolismo , Citocalasina D/farmacologia , Combinação de Medicamentos , Feminino , Geodia , Humanos , Laminina/metabolismo , Inibidores da Síntese de Ácido Nucleico/farmacologia , Proteoglicanas/metabolismo
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